ClinVar Miner

List of variants in gene LMNA reported as likely benign by Invitae

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 44
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HGVS dbSNP
NM_170707.3(LMNA):c.1071C>T (p.Asp357=) rs376875762
NM_170707.3(LMNA):c.1173C>T (p.Pro391=) rs1553265807
NM_170707.3(LMNA):c.1299C>T (p.His433=) rs61217436
NM_170707.3(LMNA):c.12G>A (p.Pro4=) rs369823958
NM_170707.3(LMNA):c.1314G>A (p.Gly438=) rs774817302
NM_170707.3(LMNA):c.1317C>T (p.Arg439=) rs374804871
NM_170707.3(LMNA):c.1381-6C>T rs371635492
NM_170707.3(LMNA):c.138C>T (p.Ile46=) rs1553261914
NM_170707.3(LMNA):c.153G>T (p.Ser51=) rs751886390
NM_170707.3(LMNA):c.1551G>A (p.Gln517=) rs41314035
NM_170707.3(LMNA):c.1609-4C>T rs1553266259
NM_170707.3(LMNA):c.1609-7C>T rs1372108861
NM_170707.3(LMNA):c.1731T>C (p.Ala577=) rs776066211
NM_170707.3(LMNA):c.1749G>A (p.Ser583=) rs970494454
NM_170707.3(LMNA):c.1770C>T (p.Thr590=) rs397517896
NM_170707.3(LMNA):c.1773C>T (p.Cys591=) rs397517897
NM_170707.3(LMNA):c.1803C>T (p.Ser601=) rs267607604
NM_170707.3(LMNA):c.1804G>A (p.Gly602Ser) rs60662302
NM_170707.3(LMNA):c.1818G>A (p.Gln606=) rs1060504514
NM_170707.3(LMNA):c.1857T>C (p.Ser619=) rs368581237
NM_170707.3(LMNA):c.1890G>A (p.Gly630=) rs770389147
NM_170707.3(LMNA):c.1912G>A (p.Gly638Arg) rs144851946
NM_170707.3(LMNA):c.192C>T (p.Thr64=) rs137969290
NM_170707.3(LMNA):c.1930C>T (p.Arg644Cys) rs142000963
NM_170707.3(LMNA):c.471G>A (p.Thr157=) rs150645079
NM_170707.3(LMNA):c.477G>A (p.Glu159=) rs1424758064
NM_170707.3(LMNA):c.513+8C>T rs1060504515
NM_170707.3(LMNA):c.643C>T (p.Leu215=) rs397517905
NM_170707.3(LMNA):c.681G>A (p.Val227=) rs769896881
NM_170707.3(LMNA):c.711T>C (p.Phe237=) rs768081358
NM_170707.3(LMNA):c.771G>A (p.Glu257=) rs1471649557
NM_170707.3(LMNA):c.789G>A (p.Leu263=) rs148557956
NM_170707.3(LMNA):c.870G>A (p.Glu290=) rs747275587
NM_170707.3(LMNA):c.895A>G (p.Ile299Val) rs150924946
NM_170707.3(LMNA):c.897C>T (p.Ile299=) rs762718963
NM_170707.3(LMNA):c.936+7C>T rs757401091
NM_170707.3(LMNA):c.937-8C>A rs751707982
NM_170707.3(LMNA):c.937-9C>T rs1332011298
NM_170707.3(LMNA):c.93G>A (p.Glu31=) rs878855235
NM_170707.3(LMNA):c.96G>A (p.Lys32=) rs775429079
NM_170707.3(LMNA):c.990G>A (p.Glu330=) rs140800215
NM_170707.4(LMNA):c.1155G>A (p.Glu385=) rs878855232
NM_170707.4(LMNA):c.1785C>T (p.Ala595=) rs748139390
NM_170707.4(LMNA):c.726G>A (p.Ala242=) rs763625309

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